Job opportunity as Regulatory Affairs professionals at BDR Pharma- Apply before 25th October 2024

BDR Pharma

Website BDR Pharma

About BDR Pharma

BDR Group of Companies has established itself as a prominent name in the pharmaceutical industry over the past 15 years. With a strong presence both domestically and internationally, we are recognized for our expertise in the manufacturing of Pharmaceutical APIs and new-age formulations. Our success is driven by two key companies: BDR Pharmaceuticals International Pvt Ltd and BDR Life Sciences Pvt Ltd, each excelling in API and formulation manufacturing, respectively.

We are currently seeking talented professionals for the following roles:


Asst Manager / Dy Manager – Regulatory Affairs (US, EU, Canada, Australia, and Brazil Markets)

Role Overview: We are looking for experienced Regulatory Affairs professionals to lead our regulatory strategy for various dosage forms, including complex injectables and ophthalmic products. The ideal candidate should have a deep understanding of CMC requirements and a proven track record in dossier review and submission for the US, EU, and Brazil markets.

  • Location: Baska, Halol
  • Experience: 5-8 years in Regulatory Affairs (Preferably US/EU Markets)
  • Qualification: M.Pharm / B.Pharm

Executive / Sr Executive – Regulatory Affairs (US, EU, Health Canada, Australia, and Brazil Markets)

Role Overview: This role is focused on managing the CMC aspects, dossier compilation, and submission processes for solid and injectable products. The successful candidate will ensure the preparation of high-quality regulatory submissions across multiple regions.

  • Location: Baska, Halol
  • Experience: 3-5 years in Regulatory Affairs (Preferably US/EU Markets)
  • Qualification: M.Pharm / B.Pharm

Officer / Sr Officer – Regulatory Affairs (US, EU, Health Canada, Australia, and Brazil Markets)

Role Overview: We are seeking candidates with up to 3 years of experience in handling CMC aspects for pharmaceutical products. This position involves dossier preparation, review, and submission in compliance with regulatory requirements for various markets, including the US, EU, and Brazil.

  • Location: Baska, Halol
  • Experience: 0-3 years in Regulatory Affairs (Preferably US/EU Markets)
  • Qualification: M.Pharm / B.Pharm

Why Join Us? At BDR Group, we offer a dynamic work environment that fosters innovation and professional growth. By joining our team, you will be part of a company that is shaping the future of the pharmaceutical industry.

Apply Today: Interested candidates are invited to send their resumes to hrd@bdrpharma.com by 25th October 2024.

Start your journey with BDR Group and make an impact in the global pharmaceutical landscape!

To apply for this job please visit bdrpharma.com.